Canonical Allele Identifier: PA2825091798
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587318
ClinVar RCV Id: RCV003360799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1186Ser
CA346760278
NM_000179.3:c.3556G>A